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Functional variants identify sex-specific genes and pathways in Alzheimer's Disease.
Bourquard T, Lee K, Al-Ramahi I, Pham M, Shapiro D, Lagisetty Y, Soleimani S, Mota S, Wilhelm K, Samieinasab M, Kim YW, Huh E, Asmussen J, Katsonis P, Botas J, Lichtarge O. Bourquard T, et al. Among authors: lee k. Nat Commun. 2023 May 13;14(1):2765. doi: 10.1038/s41467-023-38374-z. Nat Commun. 2023. PMID: 37179358 Free PMC article.
Identification of risk genes for Alzheimer's disease by gene embedding.
Lagisetty Y, Bourquard T, Al-Ramahi I, Mangleburg CG, Mota S, Soleimani S, Shulman JM, Botas J, Lee K, Lichtarge O. Lagisetty Y, et al. Among authors: lee k. Cell Genom. 2022 Sep 14;2(9):100162. doi: 10.1016/j.xgen.2022.100162. Epub 2022 Jul 26. Cell Genom. 2022. PMID: 36268052 Free PMC article.
Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease.
Pinard A, Ye W, Fraser SM, Rosenfeld JA, Pichurin P, Hickey SE, Guo D, Cecchi AC, Boerio ML, Guey S, Aloui C, Lee K, Kraemer M, Alyemni SO; University of Washington Center for Mendelian Genomics; Bamshad MJ, Nickerson DA, Tournier-Lasserve E, Haider S, Jin SC, Smith ER, Kahle KT, Jan LY, He M, Milewicz DM. Pinard A, et al. Among authors: lee k. Brain. 2023 Sep 1;146(9):3616-3623. doi: 10.1093/brain/awad172. Brain. 2023. PMID: 37253099 Free PMC article.
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